Canonical Allele Identifier: CA379962060

Gene: WT1

Linked Data

• ClinVar Variation Id: 1356875
• ClinVar RCV Id: RCV001870317
• dbSNP Id: rs2133036912
• MyVariant Identifiers: chr11:g.32439142A>T (hg19) ; chr11:g.32417596A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32417596A>T , CM000673.2:g.32417596A>T	GRCh38
NC_000011.9:g.32439142A>T , CM000673.1:g.32439142A>T	GRCh37
NC_000011.8:g.32395718A>T	NCBI36
NG_009272.1:g.22946T>A , LRG_525:g.22946T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.946T>A	ENSP00000331327.5:p.Leu316Ile
ENST00000379077.9:c.946T>A	ENSP00000368368.5:p.Leu316Ile
ENST00000379079.8:c.295T>A	ENSP00000368370.2:p.Leu99Ile
ENST00000448076.9:c.946T>A	ENSP00000413452.5:p.Leu316Ile
ENST00000452863.10:c.946T>A MANE Select	ENSP00000415516.5:p.Leu316Ile
ENST00000639563.3:c.946T>A	ENSP00000492269.3:p.Leu316Ile
ENST00000640146.2:c.322T>A	ENSP00000491984.2:p.Leu108Ile
ENST00000332351.7:c.931T>A	ENSP00000331327.3:p.Leu311Ile
ENST00000379077.7:c.931T>A	ENSP00000368368.3:p.Leu311Ile
ENST00000379079.6:c.295T>A	ENSP00000368370.2:p.Leu99Ile
ENST00000448076.7:c.931T>A	ENSP00000413452.3:p.Leu311Ile
ENST00000452863.7:c.931T>A	ENSP00000415516.3:p.Leu311Ile
ENST00000527775.1:c.184T>A	ENSP00000435351.1:p.Leu62Ile
ENST00000527882.5:c.2T>A
ENST00000530998.5:c.295T>A	ENSP00000435307.1:p.Leu99Ile
NM_000378.4:c.931T>A	NP_000369.3:p.Leu311Ile
NM_001198551.1:c.295T>A , LRG_525t2:c.295T>A	NP_001185480.1:p.Leu99Ile
NM_001198552.1:c.295T>A	NP_001185481.1:p.Leu99Ile
NM_024424.3:c.931T>A	NP_077742.2:p.Leu311Ile
NM_024426.4:c.931T>A	NP_077744.3:p.Leu311Ile
NM_000378.5:c.946T>A	NP_000369.4:p.Leu316Ile
NM_024424.4:c.946T>A	NP_077742.3:p.Leu316Ile
NM_024426.5:c.946T>A	NP_077744.4:p.Leu316Ile
NR_160306.1:n.1125T>A
NM_000378.6:c.946T>A	NP_000369.4:p.Leu316Ile
NM_001198552.2:c.295T>A	NP_001185481.1:p.Leu99Ile
NM_024424.5:c.946T>A	NP_077742.3:p.Leu316Ile
NM_024426.6:c.946T>A MANE Select	NP_077744.4:p.Leu316Ile